We typically use a media called histogel for our cytology cell blocks with very good results. Our pathologists also send us clots from other locations that they are collecting like a bone marrow aspirate clot. The FNAs are expressed into a lid and allowed to clot. We are processing these on an overnight run used for all our other cases. The histotechs are having a great deal of trouble cutting these as they are very dried out and break apart on the water bath. Is there any techniques you can recommend to get better results when cutting specimens collected this way? I would think we need to process them on a shorter program to begin with.
Thank you in advance for any suggestions. Carol Bryant, CT (ASCP) Cytology/Histology Manager Pathology Services Lexington Clinic Phone (859) 258-4082 Fax (859) 258-4081 cb...@lexclin.com NOTICE OF CONFIDENTIALITY This message, including any attachments, is intended only for the sole use of the addressee and may contain confidential or privileged information that is protected by the State of Kentucky and/or Federal regulations. If you are not the intended recipient, do not read, copy, retain or disseminate this message or any attachment. If you have received this message in error, please call the sender immediately at (859)258-4000 and delete all copies of this message and any attachment. Any unauthorized review, use, disclosure, copying or distribution is strictly prohibited. Neither the transmission of this message or any attachment, nor any error in transmission or misdelivery shall constitute waiver of any applicable legal privilege. _______________________________________________ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
